1.The authors reply.
Kidney Research and Clinical Practice 2016;35(3):193-193
No abstract available.
2.Comparison of exit site infection and peritonitis incidences between povidone-iodine and normal saline use for chronic exit site care in peritoneal dialysis patients.
Su Mi LEE ; Hwa Seong NAM ; Eu Gene JEONG ; Young Ki SON ; Seong Eun KIM ; Won Suk ANN
Kidney Research and Clinical Practice 2014;33(3):144-149
BACKGROUND: Catheter-related exit site infection is a major risk factor for the development of peritonitis and can contribute to failure of treatment maintenance in peritoneal dialysis (PD) patients. Although povidone-iodine can be used for exit site care, the irritation induced by the local application of povidone-iodine could lead to secondary infection. Therefore, we evaluated the clinical effectiveness of normal saline compared with povidone-iodine as a method of exit site care in chronic PD patients. METHODS: In all, 126 patients undergoing PD treatment for>46 months between January 2006 and December 2009 were enrolled. Data were retrospectively analyzed for the incidence of exit site infection and peritonitis for 2 years prior to and after December 2007. In addition, we identified the incidences of catheter- related infections during follow-ups from January 2010 to December 2013. RESULTS: The participants' mean age was 58.87+/-12.9 years. The incidences of exit site infection and peritonitis were one episode per 64.6 patients-months and one episode per 40.4 patients-months in the povidone-iodine group, respectively, whereas these were one episode per 57.5 patients-months and one episode per 45.6 patients-months in the normal saline group, respectively. Whereas Gram-positive bacteria most frequently caused catheter-related infections in both groups, culture-negative infections were dominant in the normal saline group. CONCLUSION: Exit site care using normal saline did not increase the incidence of exit site infection and peritonitis. Therefore, normal saline may be an alternative treatment for exit site care in patients receiving PD.
Catheter-Related Infections
;
Coinfection
;
Follow-Up Studies
;
Gram-Positive Bacteria
;
Humans
;
Incidence*
;
Peritoneal Dialysis*
;
Peritonitis*
;
Povidone-Iodine*
;
Retrospective Studies
;
Risk Factors
3.Clinicopathological role of kidney injury molecule-1 in immunoglobulin A nephropathy.
Yu Ho LEE ; Yang Gyun KIM ; Sang Ho LEE ; Ju Young MOON ; Kyung Hwan JEONG ; Tae Won LEE ; Chun Gyoo IHM
Kidney Research and Clinical Practice 2014;33(3):139-143
BACKGROUND: Urinary kidney injury molecule-1 (KIM-1) is an early and sensitive biomarker of acute kidney injury, but it is unclear if it is a biomarker of chronic glomerulonephritis. We evaluated whether urinary KIM-1 levels in patients with immunoglobulin A (IgA) nephropathy can be a marker to reflect clinicopathological severity and predict the prognosis. METHODS: We measured urinary KIM-1 levels in 40 patients (15 males; mean age 36.67+/-12.9 years) with IgA nephropathy and 10 healthy people (5 males; mean age 37.37+/-9.6 years) as controls. The correlation of urinary KIM-1 levels with patients' clinical parameters, histological grades, and follow-up data were analyzed using the modified H. S. Lee grading system and tubulointerstitial change scores. RESULTS: Urinary KIM-1 levels were higher in patients with IgA nephropathy than healthy controls (P=0.001). Univariate and multivariate regression analyses showed that urinary KIM-1 levels had a direct correlation with H. S. Lee grade and tubulointerstitial inflammation (P=0.004 and P=0.011, respectively). CONCLUSION: In patients with IgA nephropathy, urinary KIM-1 has a significant correlation with histopathologic severity.
Acute Kidney Injury
;
Follow-Up Studies
;
Glomerulonephritis
;
Glomerulonephritis, IGA*
;
Humans
;
Immunoglobulin A
;
Inflammation
;
Kidney*
;
Male
;
Prognosis
4.Chronic renal failure induces cell death in rat hippocampal CA1 via upregulation of alphaCaMKII/NR2A synaptic complex and phosphorylated GluR1-containing AMPA receptor cascades.
Jong Wan KIM ; Gyoung Yim HA ; Yong Wook JUNG
Kidney Research and Clinical Practice 2014;33(3):132-138
BACKGROUND: N-methyl-D-aspartate (NMDA) and alpha-amino-3-hydroxy-5-methyl-isoxazole-4-propinoic acid (AMPA) receptors bound to postsynaptic density-95 (PSD-95) and alpha isoform of calcium/calmodulin-dependent protein kinase II (alphaCaMKII) is fundamentally involved in the regulation of working memory. The aim of present study was to investigate the alterations of NMDA and AMPA receptors responsible for hippocampal synaptic dysfunction and selective neuronal cell death after chronic renal failure (CRF) which may be associated with impairment of working memory. METHODS: Altered interactions between NMDA and AMPA receptors and PSD-95 and alphaCaMKII were analyzed in the cornu ammonis (CA) 1 and CA3/dentate gyrus (DG) subfields of the uremic rat hippocampi using the immunoblotting and immunoprecipitation methods. RESULTS: Uremia induced by CRF produced necrotic cell death and decreased neuronal nucleoli protein levels in the hippocampal CA1 subfield, but not in the CA3/DG subfields. The CA1 subfields of CRF rats exhibited significant decreases and increases, respectively, in the expressions of PSD-95/NR2B and alphaCaMKII/NR2A synaptic complex. Moreover, increased phosphorylation of glutamate receptor type 1 (GluR1) AMPA receptor at ser831 was observed in the CA1 subfield after CRF. CONCLUSION: These hippocampal CA1 neuronal vulnerability may be responsible for memory dysfunction after CRF as mediated by an increase in NR2A-containing NMDA receptors bound to alphaCaMKII and subsequent activation of GluR1-containing AMPA receptors caused by the phosphorylation of GluR1 at ser831.
Animals
;
Cell Death*
;
Hippocampus
;
Immunoblotting
;
Immunoprecipitation
;
Kidney Failure, Chronic*
;
Memory
;
Memory, Short-Term
;
N-Methylaspartate
;
Neurons
;
Phosphorylation
;
Protein Kinases
;
Rats*
;
Receptors, AMPA*
;
Receptors, Glutamate
;
Receptors, N-Methyl-D-Aspartate
;
Up-Regulation*
;
Uremia
5.Comprehensive approach to diabetic nephropathy.
Bancha SATIRAPOJ ; Sharon G ADLER
Kidney Research and Clinical Practice 2014;33(3):121-131
Diabetic nephropathy (DN) is a leading cause of mortality and morbidity in patients with diabetes. This complication reflects a complex pathophysiology, whereby various genetic and environmental factors determine susceptibility and progression to end-stage renal disease. DN should be considered in patients with type 1 diabetes for at least 10 years who have microalbuminuria and diabetic retinopathy, as well as in patients with type 1 or type 2 diabetes with macroalbuminuria in whom other causes for proteinuria are absent. DN may also present as a falling estimated glomerular filtration rate with albuminuria as a minor presenting feature, especially in patients taking renin-angiotensin-aldosterone system inhibitors (RAASi). The pathological characteristic features of disease are three major lesions: diffuse mesangial expansion, diffuse thickened glomerular basement membrane, and hyalinosis of arterioles. Functionally, however, the pathophysiology is reflected in dysfunction of the mesangium, the glomerular capillary wall, the tubulointerstitium, and the vasculature. For all diabetic patients, a comprehensive approach to management including glycemic and hypertensive control with RAASi combined with lipid control, dietary salt restriction, lowering of protein intake, increased physical activity, weight reduction, and smoking cessation can reduce the rate of progression of nephropathy and minimize the risk for cardiovascular events. This review focuses on the latest published data dealing with the mechanisms, diagnosis, and current treatment of DN.
Albuminuria
;
Arterioles
;
Capillaries
;
Diabetic Nephropathies*
;
Diabetic Retinopathy
;
Diagnosis
;
Glomerular Basement Membrane
;
Glomerular Filtration Rate
;
Humans
;
Kidney Failure, Chronic
;
Mortality
;
Motor Activity
;
Proteinuria
;
Renin-Angiotensin System
;
Smoking Cessation
;
Weight Loss
6.Chronic exit-site care using povidone-iodine versus normal saline in peritoneal dialysis patients.
Kidney Research and Clinical Practice 2014;33(3):119-120
No abstract available.
Humans
;
Peritoneal Dialysis*
;
Povidone-Iodine*
7.The use of tacrolimus in the management of minimal change disease.
Kidney Research and Clinical Practice 2012;31(4):257-258
No abstract available.
Nephrosis, Lipoid
;
Tacrolimus
8.A case of membranous nephropathy associated with relapsing polychondritis.
Kidney Research and Clinical Practice 2012;31(4):253-256
Relapsing polychondritis (RP) is a rare, chronic, and potentially fatal multisystemic inflammatory disorder targeting cartilaginous structures. This disorder is frequently associated with rheumatoid arthritis, systemic vasculitis, connective tissue diseases, and hematologic disorders, but renal involvement is unusual. In the literature, associated renal pathology includes mesangial expansion, IgA nephropathy, tubulointerstitial nephritis, and segmental necrotizing crescentic glomerulonephritis. We report a case of a 49-year-old male found to have RP and nephrotic syndrome, with confirmed membranous nephropathy on kidney biopsy. He responded well to corticosteroids and cyclosporine. This is the first case of renal associated RP confirmed by renal biopsy in Korea. Membranous nephropathy associated with RP has never before been reported.
Adrenal Cortex Hormones
;
Arthritis, Rheumatoid
;
Biopsy
;
Connective Tissue Diseases
;
Cyclosporine
;
Glomerulonephritis
;
Glomerulonephritis, IGA
;
Glomerulonephritis, Membranous
;
Humans
;
Kidney
;
Korea
;
Male
;
Nephritis, Interstitial
;
Nephrotic Syndrome
;
Polychondritis, Relapsing
;
Systemic Vasculitis
9.Acute oxalate nephropathy caused by ethylene glycol poisoning.
Jung Woong SEO ; Jong Ho LEE ; In Sung SON ; Yong Jin KIM ; Do Young KIM ; Yong HWANG ; Hyun Ah CHUNG ; Hong Seok CHOI ; So Dug LIM
Kidney Research and Clinical Practice 2012;31(4):249-252
Ethylene glycol (EG) is a sweet-tasting, odorless organic solvent found in many agents, such as anti-freeze. EG is composed of four organic acids: glycoaldehyde, glycolic acid, glyoxylic acid and oxalic acid in vivo. These metabolites are cellular toxins that can cause cardio-pulmonary failure, life-threatening metabolic acidosis, central nervous system depression, and kidney injury. Oxalic acid is the end product of EG, which can precipitate to crystals of calcium oxalate monohydrate in the tubular lumen and has been linked to acute kidney injury. We report a case of EG-induced oxalate nephropathy, with the diagnosis confirmed by kidney biopsy, which showed acute tubular injury of the kidneys with extensive intracellular and intraluminal calcium oxalate monohydrate crystal depositions.
Acidosis
;
Acute Kidney Injury
;
Biopsy
;
Calcium Oxalate
;
Central Nervous System
;
Depression
;
Ethylene Glycol
;
Ethylenes
;
Glycolates
;
Glyoxylates
;
Kidney
;
Oxalic Acid
10.Bilateral gluteal compartment syndrome complicated by rhabdomyolysis and acute kidney injury in a patient with alcohol intoxication.
Jae Young CHO ; Jae Won LEE ; Eun Jung CHO ; Myung Gyu KIM ; Sang Kyung JO ; Won Yong CHO ; Hyoung Kyu KIM
Kidney Research and Clinical Practice 2012;31(4):246-248
Bilateral gluteal compartment syndrome is a rare clinical entity that can be complicated by rhabdomyolysis or acute kidney injury (AKI). We report the a case of a 30-year-old woman without any comorbid diseases who was diagnosed with bilateral gluteal compartment syndrome complicated by rhabdomyolysis and dialysis-requiring AKI, which was caused by prolonged immobilization under the influence of alcohol. Although the patient's renal function recovered fully after 5 sessions of hemodialysis, sciatic neuropathy caused by gluteal compartment syndrome led to permanent foot drop.
Acute Kidney Injury
;
Alcoholic Intoxication
;
Compartment Syndromes
;
Female
;
Foot
;
Humans
;
Immobilization
;
Renal Dialysis
;
Rhabdomyolysis
;
Sciatic Neuropathy